The hydrogen storage performance and catalytic mechanism of the MgH2 -MoS2 composite

被引:25
作者
Wang, Luxiang [1 ,2 ,3 ]
Hu, Yiwanting [1 ,2 ,3 ]
Lin, Jiayu [1 ,2 ,3 ]
Leng, Haiyan [1 ,2 ,3 ]
Sun, Chenghua [4 ]
Wu, Chengzhang [1 ,2 ,3 ]
Li, Qian [1 ,2 ,3 ,5 ]
Pan, Fusheng [5 ]
机构
[1] Shanghai Univ, State Key Lab Adv Special Steel, Shanghai 200444, Peoples R China
[2] Shanghai Univ, Shanghai Key Lab Adv Ferromet, Shanghai 200444, Peoples R China
[3] Shanghai Univ, Sch Mat Sci & Engn, Shanghai 200444, Peoples R China
[4] Swinburne Univ Technol, Fac Sci Engn & Technol, Ctr Translat Atomat, Hawthorn, Vic 3122, Australia
[5] Chongqing Univ, Coll Mat Sci & Engn, Natl Engn Res Ctr Magnesium Alloys, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen storage; Magnesium hydride; MoS; 2; Evolution; Catalytic mechanism; MAGNESIUM HYDRIDE; DESORPTION-KINETICS; MOS2; MICROSTRUCTURE; NANOPARTICLES; ABSORPTION; SORPTION;
D O I
10.1016/j.jma.2022.06.001
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
In this work, we synthesized MoS 2 catalyst via one-step hydrothermal method, and systematically investigated the catalytic effect of MoS 2 on the hydrogen storage properties of MgH 2 . The MgH 2 -5MoS 2 composite milled for 5 h starts to release hydrogen at 259 & DEG;C. Furthermore, it can desorb 4.0 wt.% hydrogen within 20 min at 280 & DEG;C, and absorb 4.5 wt.% hydrogen within 5 min at 200 & DEG;C. Mo and MoS 2 coexisted in the ball milled sample, whereas only Mo was kept in the sample after dehydrogenation and rehydrogenation, which greatly weakens the Mg-H bonds and facilitates the dissociation of MgH 2 on the surface of Mo (110). The comparative study show that the formed MgS has no catalytic effect for MgH 2 . We believed that the evolution and the catalytic mechanism of MoS 2 will provide the theoretical guidance for the application of metal sulfide in hydrogen storage materials. & COPY; 2022 Chongqing University. Publishing services provided by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ ) Peer review under responsibility of Chongqing University
引用
收藏
页码:2530 / 2540
页数:11
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